A straightforward protocol for the synthesis of a previously unknown [1,2,5]oxadiazolo[3,4-][1,2,3]triazin-7(6)-one heterocyclic system was developed. The described approach is based on tandem diazotization/azo coupling reactions of (1,2,5-oxadiazolyl)carboxamide derivatives bearing both aromatic and aliphatic substituents. The NO-donor ability of the synthesized furoxano[3,4-][1,2,3]triazin-7(6)-ones was additionally evaluated. The elaborated method provides access to novel nitrogen heterocyclic compounds with potential applications as drug candidates or thermostable components of functional organic materials.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11420545PMC
http://dx.doi.org/10.3762/bjoc.20.200DOI Listing

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